胰岛素瘤细胞系Rin-5F中yes相关蛋白1 (YAP1)突变状态

IF 1.4 4区 医学 Q4 GENETICS & HEREDITY
Takayoshi Kiba
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引用次数: 0

摘要

先前的研究表明,YAP1突变可以增强对免疫检查点抑制剂的反应,并且这种突变可以通过增加突变计数作为对各种癌症免疫治疗反应的新预测因子。分泌胰岛素的胰腺细胞系Rin-5F常用于药理学和毒理学研究。在本研究中,作者利用来自Rin-5F细胞的基因组DNA和互补DNA检测了YAP1基因的突变。目前的研究未发现YAP1基因突变。YAP1基因在胰岛素瘤细胞系中的地位以前没有文献记载。根据先前的研究,YAP1突变可能与免疫检查点抑制剂的增强反应有关。鉴于该胰岛素瘤细胞系中没有YAP1基因突变,免疫检查点抑制剂对胰岛素瘤的影响可能会降低。为了解决这个问题,免疫检查点抑制剂需要进一步的临床试验用于神经内分泌肿瘤,如胰岛素瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mutation status in yes-associated protein 1 (YAP1) in an insulinoma cell line Rin-5F
Previous research indicates that YAP1 mutations may enhance responses to immune checkpoint inhibitors, and this mutation could serve as a novel predictor of response to immunotherapy across various cancers by increasing mutation counts. The insulin-secreting pancreatic cell line Rin-5F is commonly used in pharmacological and toxicological studies. In the present study, the author has examined mutations in the YAP1 gene using genomic DNA and complementary DNA from Rin-5F cells. No mutations in the YAP1 gene were identified in the current investigation. The status of the YAP1 gene in an insulinoma cell line has not been previously documented. According to previous research, YAP1 mutations may be associated with enhanced responses to immune checkpoint inhibitors. Given that there is no mutation of the YAP1 gene in this insulinoma cell line, it is possible that immune checkpoint inhibitors may have a reduced impact on insulinoma. To address this question, further clinical trials of immune checkpoint inhibitors are needed for neuroendocrine tumors, such as insulinomas.
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来源期刊
Cancer Genetics
Cancer Genetics ONCOLOGY-GENETICS & HEREDITY
CiteScore
3.20
自引率
5.30%
发文量
167
审稿时长
27 days
期刊介绍: The aim of Cancer Genetics is to publish high quality scientific papers on the cellular, genetic and molecular aspects of cancer, including cancer predisposition and clinical diagnostic applications. Specific areas of interest include descriptions of new chromosomal, molecular or epigenetic alterations in benign and malignant diseases; novel laboratory approaches for identification and characterization of chromosomal rearrangements or genomic alterations in cancer cells; correlation of genetic changes with pathology and clinical presentation; and the molecular genetics of cancer predisposition. To reach a basic science and clinical multidisciplinary audience, we welcome original full-length articles, reviews, meeting summaries, brief reports, and letters to the editor.
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